Actively Recruiting

Phase Not Applicable
Age: 21Years +
All Genders
NCT07027709

Clinical Performance of Hybrid Ceramic Laminate Veneers

Led by Cairo University · Updated on 2025-06-18

28

Participants Needed

1

Research Sites

82 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized controlled trial evaluates the clinical performance of laminate veneers fabricated from HC hard blocks pretreated with BeautiBond Xtreme versus HC Primer, using BeautiLink SA cement. The study focuses on marginal adaptation, retention, discoloration, and recurrent caries over 18 months.

CONDITIONS

Official Title

Clinical Performance of Hybrid Ceramic Laminate Veneers

Who Can Participate

Age: 21Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients aged 21 years or older requiring laminate veneers in the esthetic zone
  • Teeth may be vital or endodontically treated
  • Sufficient enamel present on teeth
  • Willing and able to give consent and comply with study procedures
Not Eligible

You will not qualify if you...

  • Presence of periodontal disease
  • Bruxism (teeth grinding)
  • Poor oral hygiene
  • Pregnancy
  • Systemic illness
  • Allergies to dental materials
  • Insufficient enamel on teeth
  • Participation in other clinical trials
  • Currently receiving orthodontic treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Faculty of Dentistry Cairo University

Cairo, Egypt

Actively Recruiting

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Research Team

O

omnia Mohammed Wafik, lecturer

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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